Abstract
Marsh edge retreat by wave erosion, an ubiquitous process along estuaries, could affect vegetation dynamics in ways that differ from well-established elevation-driven interactions. Along the marshes of Delaware Bay (USA) we show that species composition from marsh edge to interior is driven by gradients in wave stress, bed elevation, and sediment deposition. At the marsh edge, large wave stress allows only short-statured species. Approximately 17m landward, decreasing wave stress and increasing deposition cause the formation of a ridge. There, high marsh fugitive and shrub species prevails. Both the marsh edge and the ridge retreat synchronously by several meters per year causing wave energy and deposition to change rapidly. Yet, the whole ecogeomorphologic profile translates landward in a dynamic equilibrium, where the low marsh replaces the high marsh ridge community and the high marsh ridge community replaces the mid-marsh grasses on the marsh plain. A plant competition model shows that the disturbances associated with sediment deposition are necessary for the high marsh species to outcompete the mid-marsh grasses during rapid transgression. Marsh retreat creates a moving framework of physical gradients and disturbances that promote the co-existence of over ten different species adjacent to the marsh edge in an otherwise species-poor landscape.
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Introduction
Coastal marshes are a transitional ecosystem between the land and the sea, providing a number of important ecological services including habitat for ecologically and economically important species, sequestration of carbon and other pollutants, and coastal protection1. In a regime of rising sea-level and anthropogenic modifications, however, marshes are increasingly experiencing deterioration and loss. Even in the absence of sea-level rise, mature salt marshes, which tend to slope steeply to the intertidal flat, are being lost due to inherent lateral retreat by wave-induced edge erosion2,3. As marshes retreat laterally, low marsh plant species are predicted to migrate landward at the expense of mid- and high marsh species, particularly in areas with barriers to inland migration4,5. Loss of high marsh species at the upland boundary can significantly lower overall vegetation diversity and complexity, as low elevations tend to be dominated by one or a few stress-tolerant species.
Coastal wetlands are ideal systems to test hypotheses of drivers of plant community patterns due to strong gradients in abiotic conditions, relatively low species richness, and striking plant zonation6,7,8. Plant community dynamics in salt marshes have been determined primarily for the relatively stable marsh interior, where discrete disturbances are infrequent. In the marsh interior, competitive interactions tend to increase as tidal flooding and salinity decline, generally regulated by elevation8,9,10. Less competitive, stress-tolerant species, such as Spartina alterniflora, are relegated to frequently-flooded low marsh elevations by competitive exclusion by mid-marsh species such as Spartina patens8,10. Similarly, high marsh shrubs are limited by the physical stresses at lower elevations and outcompete marsh grasses in areas of reduced flooding11,12. Therefore, sea-level rise and increased inundation generally causes the replacement of mid- and high marsh species with low marsh grasses13,14.
An exception to the paradigm of elevation-driven competition might be present at the marsh-estuary boundary, where physical processes due to waves create frequent disturbances that may affect plant community structure and species interactions15. Waves directly shear the vegetation and rework the soil surface, an effect that is greatest at the marsh edge and declines exponentially inland16. Waves also have an indirect effect of depositing sediments and plant debris (i.e., wrack), which can smother existing plants17,18 and provide opportunities for rapid colonization by fugitive and high marsh species sensu8,19. Along these high-energy marsh shorelines, frequent wave-induced disturbances along with gradients in elevation may control vegetation patterns, whereby community structure and species diversity depend on the frequency and intensity of disturbances, species-specific growth rates, and niche preferences20. These interactions, however, have yet to be described or modeled for high-energy marsh edge environments.
At the estuary-marsh transition, physical disturbances are also compounded by a retreating marsh edge boundary, which forces the vegetation to rapidly adapt to changing physical conditions. This setting contrasts with the channel-interior marsh boundary, which remains relatively stable over time and only varies gradually with sea-level rise. Given that rates of marsh edge retreat can be up to 10 meters per year21,22present study (Table S1), it is unclear whether the vegetation near the marsh edge is simply lost in succession or adapts. With the inherent retreat of marsh boundaries when sediment input is less than what is eroded2,3, characterizing linkages between vegetation patterns and underlying morphodynamics is essential for a mechanistic understanding of succession and species movement patterns in rapidly changing estuary-marsh landscapes.
With this study, we aimed to examine how intense physical drivers interact with biotic interactions to influence vegetation structure (i.e., species composition, richness, height, and density) along a rapidly retreating the marsh-estuary boundary. A simple plant competition model was developed to explain field observations that included both physical disturbances and interactions among species. Previous models have simulated competition between multiple salt marsh plant species23,24, but have not accounted for physical disturbances other than those associated with inundation. In addition, previous plant competition models23,24,25 have assumed that the parameters driving the stochastic vegetation dynamics adapt instantaneously to the relative fitness, an assumption that might not hold where ecotones are migrating at extremely fast rates (e.g., >10 m yr−1).
Dynamics of The Marsh Edge and Marsh Ridge
The Delaware Estuary is a mesotidal drowned valley undergoing marine transgression as a result of relative sea level rise, which in the last century has averaged 3.5 mm y−1 26. The fringing marshes bordering the estuary are characterized by a steep scarp that – subject to energetic swell and sea waves – has been retreating at a rate of 1.2 ± 0.1 m y−1 over the long-term (1879–2012) and 2.8 ± 0.5 m y−1 more recently (2007–2012)27. Marsh edge erosion, which is common in marshes around the world, has here created a prominent feature: a 0.47 ± 0.02 m high and 3–10 m wide wash-over ridge bordering much of the wetland-dominated lower estuary (Figs 1 and 2).
Field observations indicate that the ridge is composed primarily of fine sand resuspended from the tidal flat and secondarily of stem fragments of Phragmites australis (i.e., wrack); rarely did any muds of marsh origin accumulate. Bay-wide estimates from 2017 indicate that the sediment ridge averaged 17.5 ± 0.3 m from the marsh edge (Fig. 1D). The average occurrence of the ridge at approximately 17 m is supported by field data, where only small quantities of sediment accumulated at plots originating 5 m from the marsh edge (48 ± 36 kg m−2 yr−1), while sediment deposition was an order of magnitude greater at 15 m (464 ± 234 kg m−2 yr−1; Fig. S1). This location was characterized by large episodic deposition events including 8,058 kg m−2 of wrack and sediment (60% organic matter by weight) between March and May 2015 and 47,580 kg m−2 of fine sand between May and August 2016, the latter equivalent to over 1 m of sediment accretion (Figs 3 and S2). Similarly, surface accretion rate was over 7 times greater at a 15 m distance (7.6 ± 3.5 cm yr−1) than 5 m from the marsh edge (<1 cm yr−1; Fig. S1).
At the estuary-scale, the ridge migrated landward at a rate close to the rate of marsh edge retreat over a range of 0 to 15 m yr−1 (Fig. 1C), indicating near instantaneous adaptation of the ridge to wave erosion and sediment deposition. Although the distance between the marsh edge and the ridge remained nearly constant at each location over time, the distance varied spatially within the estuary from 10 to about 40 m (Fig. 1D). The distance of the ridge from the marsh edge was not correlated with the rate of marsh edge retreat or with the orientation of the coastline (Fig. 1D).
Plant community patterns
Vegetation within approximately 10 m of the marsh edge was either sheared or comprised of short-statured stress-tolerant, S. alterniflora (Figs 2 and 3C). The occurrence of S. alterniflora close to the marsh edge demonstrates the ability of this species to withstand not only frequent flooding at low elevations, but also the direct physical stresses imposed by waves. At approximately 15 m distances, an abrupt change in vegetation is represented by a reduction in S. alterniflora, and the novel occurrence of high marsh and fugitive species including Atriplex patula, Bolboschoenus robustus, Iva frutenscens, P. australis, Solidago sempervirens, and Spartina cynosuroides (Figs 2, 3; Figs S1, S3 and S4) – plant species that are typically found seaward of the terrestrial border or along levees or drainage ditches. Iva frutescens, for example, is found at elevations of 1.5 m above mean sea level or where water tables average greater than 10 cm depth11. Similarly, P. australis is limited to colonizing high marsh habitats with low soil salinities and high soil oxygen levels28. In the Delaware Estuary, high marsh species other than those present on the ridge are generally located in the high marsh/upland boundary more than several km away from the marsh edge.
In order to concisely quantify the vegetation pattern, we calculated the Vegetation Structure Index (VI) as the product of species richness, mean canopy height, and stem density after29. This parameter gives intentional weight to changes in the number of species, and similarly reflects the dynamics of each structural component (Fig. S5). Abrupt changes in vegetation structure (VI) and species composition coincided with wave-driven changes in topography and sediment deposition over time (Fig. 3). Spartina alterniflora was more frequent, taller, and denser closer to the marsh-estuary boundary, where elevations and deposition rates were lower (Fig. 3). High marsh species had high VI around 15 m from the edge, where elevation and deposition rates were higher (Fig. 3).
High elevations created by sediment deposits are also accompanied by a disturbance effect where deposition eliminates competition and creates an open niche allowing the opportunistic colonization of high marsh perennials, annuals, and fugitive species. Ridge transgression, therefore, initiates a sequence of ecological succession with the colonization of S. alterniflora at the abandoned seaward edge where high marsh species are lost due to wave exposure, smothering of mid-marsh grasses on the landward edge of the ridge, and colonization and persistence of high marsh species on the ridge.
Vegetation structure was also influenced by lateral marsh retreat. For both S. alterniflora, which was dominant at 0 and 5 m from the edge, and high marsh species, which were dominant 15 m from the edge (i.e., on the ridge), VI was variable, but generally high, for rates of edge erosion of <2 m yr−1 and very low for lateral retreat rates of >8 m yr−1 (Figs S6 and S7). Despite the loss of vegetation close to the edge, distinct zones of species were maintained even where the retreat rates were so high (up to 14 m yr−1, Fig. 1) that the whole ridge was replaced within one year. Thus, high rates of marsh retreat did not cause a progressive loss of vegetation, but rather triggered an inland migration of the ridge and associated plant communities.
Model of marsh morphodynamics and plant species interactions
To investigate the importance of gradients in physical stress and the disturbance of sedimentation events on plant species interactions, we developed a simple ecogeomorphic model. The model simulates a shore-normal transect across the marsh platform starting from the marsh edge, which migrates landward at a rate M (m yr−1). The evolution of the elevation z is described by a balance between wave erosion, E, and deposition, D, as \(\dot{z}=D-E\) (Fig. 4A). The erosion term E is equal to a constant value up to the distance L from the marsh edge and then becomes zero, simulating the rapid decay of wave action away from the marsh edge. Because waves are only able to erode newly deposited sediment above the marsh platform but not the consolidated sediment, wave erosion only takes place up to the elevation zbase, which is set equal to the low marsh elevation. The deposition term D is zero up to distance L and then increases to a value of Do, followed by an exponential decay at a rate α. Do is set equal to the edge erosion rate, M, multiplied by a constant factor β, which describes the amount of material that is conserved and locally redeposited as the marsh retreats. Noticeably, the factor β should be close to zero in the presence of muddy sediment, which once eroded is quickly transported away, whereas it should be closer to one in the presence of sandy sediment, which redeposits close to the location it is eroded from.
Following a previous model for multi-species marsh plant competition as a function of elevation23, we introduce the elevation fitness function,\({f}_{i}=2/(exp({\lambda }_{i}z/(z-z{o}_{i}))+exp(\,-\,{\lambda }_{i}z/(z-z{o}_{i})))\) where zoi is the optimum elevation for the species i, and λi defines the spreading of the fitness function with elevation (Fig. 4B,C). The wave disturbance effect (causing plant shearing and breakage) is introduced by setting the vegetation fitness equal to zero in areas where wave erosion takes place (i.e., where E > 0) for stress-intolerant species, such as S. patens and high marsh shrub species9 (Fig. 4A).
The evolution of the normalized vegetation biomass, Xi, stems from growth, set proportional to the relative fitness \({f}_{i}/[{\sum }_{j}{f}_{j}]\), and decay, set proportional to Xi. The governing equation thus reads \(\mathop{{X}_{i}}\limits^{\cdot }=1/k({f}_{i}/[{\sum }_{j}{f}_{j}]-{X}_{i})\), where k is the adaption time (yr), which is the time scale needed for plants to adapt to the relative fitness. Adaptation time can also be considered as the inverse of the normalized growth rate, which is the growth rate (biomass/time) divided by the asymptotic value (biomass at steady state). According to this simple model, when the adaption time is short, the vegetation quickly approaches steady state, which is characterized by Xi equal to \({f}_{i}/[{\sum }_{j}\,{f}_{j}]\). The limit case of k equal to zero is equivalent to the model of Marani et al. (2013): plants have no residual fitness from the previous year and their biomass – or the expected value of the biomass if a stochastic model is considered23 – adapts instantaneously to the present fitness conditions. If the adaption time is long, the vegetation has memory and its biomass reflects the biomass of the previous year. As a reference, the adaption time is set equal to one year, which means that a newly seeded plant (with no memory of the past season, e.g., without roots and rhizomes) reaches 63% of the steady state biomass within a year and 87% of the steady state biomass within two years.
To contextualize the model with the Delaware Bay system, the parameter L was set equal to the distance between the marsh edge and the ridge (~15 m, Fig. 1D), the parameter β was set equal to 0.5 to match observed deposition rates, the decay rate for the deposition was set equal to 0.5 m−1 to reproduce the observed ridge width based on LiDAR data. Edge erosion M was 1–20 m yr−1, depending on the model simulation, resulting in Do values of 0.5 to 10 m yr−1. Edge erosion rates of 2 m yr−1, representative of historical to recent rates of edge erosion27, resulted in a Do value of 1 m yr−1, which matches the maximum accretion rate measured at the ridge. E was set equal to 3 m yr−1 to match the seaward geometry of the ridge. Vegetation parameters were chosen to match field observations and mirror previous models23: optimal elevation for S. alterniflora was set to be between MSL and the low marsh elevation (0.6 m above MSL), optimal elevation for S. patens was set equal to the elevation of the mid-marsh platform (1.1 m above MSL), and the optimal elevation for shrubs was set to 1.5 m above MSL11 (Fig. S7). The spreading parameter, λ, was set to 10 (unitless).
Model Results and Discussion
The model recreates a bulldozer-like effect, where the whole edge-platform-ridge profile migrates landward in a dynamic equilibrium, similar to a previous model for eolian dune migration30. The rapid transgression of marsh topography requires quick adaptation of the vegetation to preserve the floral zones as a cohesive unit e.g.,15. In both the low marsh and the marsh plain, the vegetation matches the local fitness: the low marsh is dominated by S. alterniflora as waves remove stress-intolerant plants, whereas the marsh plain is dominated by S. patens, which has a competitive advantage over stress-tolerant species (Fig. 4D). Noticeably, the vegetation on the ridge deviates from the local fitness, i.e., S. patens dominates over the shrub species despite the latter having higher fitness at that elevation. This arises from the time limitation for shrubs to colonize the ridge when in competition with S. patens prior to experiencing the effect of edge retreat and thus succumbing to wave stresses (Fig. 4E). In order for the shrub community to dominate on the ridge, the adaption time needs to be shorter, e.g., to 0.1 yr, thus allowing rapid colonization and establishment (Fig. 4E).
We suggest that this shorter adaption time is provided by the wave disturbance. Specifically, we suggest that sediment deposition eliminates or reduces interspecific competition with dense perennial grasses, thus allowing new high marsh species to colonize the ridge more readily. Indeed, newly deposited sandy sediment provides a well-drained substrate which can be readily colonized by high marsh plants, while wrack smothers existing plants and traps additional sediments before colonization. Multiple processes including vegetative colonization, stochastic dispersal, seedling establishment, and competition must occur on time-scales shorter than ridge migration. In general, disturbances tend to favor colonization by seed31 and create increased resource availability (e.g., higher light levels) favorable to seed germination and seedling emergence for many species32,33. Species such as P. australis, an invasive grass, often found at the high marsh – upland transition, readily exploits these disturbances due to its prolific seed production34, widespread seed dispersal35, and persistence in the seed bank36. Similarly, the spread of P. australis both along the shoreline37 and in the high marsh19 has been attributed to sediment and/or wrack deposition that elevate the substrate above mean high water38. These model results agree with previous studies that have shown that sediment deposition events can stimulate low marsh grass productivity only up to an approximate threshold depth of 30 cm; above this threshold mortality occurs thus allowing the colonization of high marsh species via seed dispersal and seedling recruitment39,40.
Noticeably, the effect of wrack deposition on the ridge differed from what is commonly observed in the marsh interior. Wrack deposited in the marsh interior smothers extant vegetation and can trigger a loss of elevation and soil carbon41. Following eventual wrack decay, vegetation succession may begin with the initial colonization of salt tolerant species8 or, alternatively, ponds may form42,43. On the contrary, at the marsh edge, wrack was generally admixed with sand deposits resulting in an alternative ecological trajectory where the ridge substrate provided relatively porous, aerated conditions that promoted the rapid decay of wrack and colonization of high marsh species. Thus, the combined effect of sand and wrack deposition on the ridge was to accelerate colonization by fugitive and high marsh plants.
Finally, even in the presence of disturbances (i.e., short adaption time), very fast rates of marsh retreat (20 m yr−1) resulted in lower shrub biomass on the ridge and lower S. alterniflora biomass in front of the ridge (Fig. 5). This result agrees with the field observations of low vegetation structure in areas with the fastest edge retreat rates (Fig. S6). This finding also supports the idea that in the presence of fast changing physical conditions, plant biomass (or the expected value of the biomass) is not necessarily in equilibrium with the local fitness as assumed in previous models23. For example, the model predicts that for extremely fast rates of marsh edge retreat (30 m yr−1), high marsh species would not be able to colonize the ridge.
Parameterizing the effect of disturbances by modifying the adaption time is a simple and efficient approach to simulate complex ecological interactions. This approach might complement the “windows of opportunity” approach, which recently has been successfully applied to simulate the encroachment of Spartina on the bare mudflat facing the marsh edge44. The adaption time approach can be useful in other ecotones with different types of competing plant species (e.g., marshes vs mangroves, or mangroves vs terrestrial vegetation) and different physical disturbances (e.g., episodic flooding, salinity, droughts, fires, and diseases).
Importantly, our observations and model results support existing theories explaining patterns of species richness and niche separation. Low species richness or outright mortality is predicted to correspond to a high frequency and intensity of disturbances, particularly where environmental stress is also high45, similar to conditions at the marsh edge. Wave disturbance weakens and abiotic stress declines with increasing distance from the marsh edge, increasing the potential for species interactions and increasing the number of possible species. In the absence of sediment deposition and ridge formation, which is predicted by the model in the case of β equal to zero (i.e., in the absence of sand re-deposition), low marsh species would directly transition to mid-marsh grasses as the result of competitive exclusion. Model results contribute to mounting support that disturbances increase the rate of competitive exclusion e.g.,46, in this case, by allowing rapid colonization and competitive exclusion of ridge species over mid-marsh grasses. The maintenance of these vegetation zones, albeit in non-equilibrium with the local fitness as the marsh edge and ridge migrate landward, is a function of metacommunity dynamics where localized disturbance, dispersal ability, and rapid growth rates facilitate the near-continuous re-colonization of the retreating marsh edge and ridge. The ridge community is comprised of fugitive species, which are poor competitors but efficient colonizers, as well as high marsh species, which are competitively-dominant. Overall, the combination of frequent disturbances and a strong abiotic gradient (i.e., elevation) provides temporal niche opportunities for spatial differentiation among species creating a relatively diverse co-existence of species in an otherwise species-poor environment47.
Conclusions
Waves are agents of recurrent catastrophic (vegetation removal) and non-catastrophic (vegetation stress) disturbances. In Delaware Bay, energetic waves and sand availability on the intertidal flat create sharp gradients in physical-sedimentary disturbances within 20 m of the marsh edge. These gradients structure the vegetation community into distinct zones that differ from the gradual elevation-driven zonation exhibited in the marsh interior. An abrupt shift in species composition occurs where bed stresses reduce wave energy and sediments fall out of the water column. There, stress-tolerant species shift to competitive high marsh species. The reduction in the plant adaption time associated with the deposition disturbances allow the high-marsh plant community to colonize the ridge during the relatively short time period between formation and destruction of the ridge.
Sea-level rise and marsh edge erosion have the potential to cause net marsh loss as well as replacement of high marsh habitat with low marsh habitat, especially where the marsh is subject to coastal squeeze and is impeded to transgress inland. This loss of high marsh habitat reduces the overall diversity and complexity of the marsh vegetation community, potentially leading to negative effects on wildlife species that depend on high marsh habitat (e.g.)48. In Delaware Bay, edge erosion is occurring more rapidly than landward transgression of the marsh into upland habitat49, indicating that high marsh species at the upland border may be lost. Here, we show that the presence of ridge near the marsh edge creates a novel high marsh habitat in an otherwise low marsh landscape. The disturbance associated with wave deposition allows rapid colonization of fugitive and high marsh species, allowing this community to transgress landward in dynamic equilibrium with the rapidly moving landscape. Thus, while the process of edge erosion is causing a net marsh loss, a high marsh habitat is created and maintained, providing a diverse and accessible habitat for wetland biota.
Materials and Methods
The Delaware Estuary is a drowned valley of the Delaware River extending approximately 200 km from the mouth at Cape May, NJ to the head of tide at Trenton, NJ. The Estuary is characterized by semidiurnal tides with a tidal range that is amplified up-estuary from approximately 1.5 m at the mouth to approximately 3.0 m in Trenton, NJ. Sea-level rise rates averaged 3.5 mm per year over the last century due to a combination of eustatic sea-level rise and post-glacial subsidence26. While hard structures border much of the upper urban corridor from Wilmington, Delaware to Trenton, New Jersey, the middle and lower estuary is bordered primarily by tidal marshes and creeks interspersed with sandy beaches. Delaware Bay wetlands formed over unconsolodated Pleistocene sediments during Holocene sea level rise, and have since switched from constructive to destructive50. Wave activity at the edge of the tidal wetlands erodes the aggraded Holocene marsh and builds migrating sandy washover barriers51. Remote images and LiDAR show a characteristic sediment ridge on the marsh surface ringing much of the wetland-dominated lower estuary (Fig. 1). To characterize the location and distance of the sediment ridge from the marsh edge and determine relationships between ridge migration and marsh edge erosion, satellite images from 1991 and 2017 were used.
A field investigation was conducted to examine relationships between vegetation structure and composition and lateral erosion and sediment deposition along two >2 km stretches of marsh shoreline experiencing relatively high rates of long-term retreat (>5 m yr−1) on opposite sides of the Delaware Estuary. Bombay Hook (BH) on the western shore included the mouth of the Leipsic River in Bombay Hook National Wildlife Refuge and Stow Creek (SC) on the eastern shore included the mouth of Stow Creek. Stow Creek is near the estuarine turbidity maximum zone, which extends 70–120 km up-estuary where both suspended sediment concentrations and mudfloc sizes can be larger than areas up- and downstream52. The transition from tidal flat to marsh was variable alongshore, showing stepped profiles, erosional cliffs, undercutting, gentle and steep slopes, tidal gullies and islands.
At each study location, five transects perpendicular to the shoreline were established from approximately 10 m seaward to 15 m landward of the marsh edge. RTK surveys were repeatedly conducted along transects to examine changes in marsh edge profiles over a two-year period. Repeated GPS surveys of marsh profiles were conducted using a Leica GS 14 (Geoid 12 A coordinate system DE NAD83). Latitude, longitude and elevation data were collected approximately every 2.5 m along five transects from the intertidal flat to a 15 m distance into the marsh in July 2014, May and October 2015, and July and October 2016.
Lateral erosion rates at three depths on the marsh scarp were measured by use of erosion pins constructed of 2 m long rebar welded to square plates. Erosion pins were inserted horizontally at the live root zone (5 cm below the surface), below the root zone characterized by fine grained muds and well decomposed organic matter, and approximately 65–100 cm below the marsh surface and ~25 cm above the tidal flat (base). Measurements were made from the base of pin head to the marsh edge on each of the four sides over 827 days. In the event of erosion pin loss, RTK measurements of changes in marsh profile were used to estimate erosion. Erosion rates were calculated based on significant regressions of marsh edge movement for each pin.
Permanent vegetation and marker horizon plots were established at the marsh edge (0 m), and 5 and 15 m distances landward from the marsh edge. Plant species cover and height, and stem density were measured in 0.25 m2 permanent plots at 0, 5, and 15 m from the marsh edge along each transect. Measurements were made seven times from July 2014–2016. For analysis, a vegetation structure index (VI) was calculated as the product of species richness, stem density, and average canopy height29. This multiplicative calculation method was chosen due to its sensitivity to the number of species53. Because salt marshes are largely monospecific, we were interested in reflecting the weight of increasing species richness to the overall vegetation structure (vs. just simply measures of biomass − height × density). VI was calculated separately for the stress-tolerant species near the marsh edge, S. alterniflora, and the high marsh and fugitive species. Feldspar marker horizons were installed in July 2014 in 50 × 50 cm plots following the methodology of 28. Vertical accretion was measured as the change in height above the marker along three sides of a square plug cut from the plot. Accretion measurements were collected up to seven times from July 2014 to October 2016. Sediment deposition on the marsh surface was measured at 5 and 15 m from the edge by use of 15.5 cm2 aluminum sediment plates welded to anchor poles inserted vertically into the marsh. Care was taken to adjust the surface of plates flush with the marsh surface. Sediment deposited on the plates was collected seven times from July 2014 to October 2016, at two to four month intervals.
Data analysis
Linear regression analysis were used to test the relationships between distance from the marsh edge, elevation, sediment deposition rate, and vegetation indices. Erosion rate data were natural log-transformed prior to statistical analysis. The influence of erosion, elevation, and sediment deposition rates on VI of were tested using regression analysis.
Data Availability
All data generated and analyzed during this study are included in this published article (and its Supplementary Information files).
References
Barbier, E. B. et al. The value of estuarine and coastal ecosystem services. Ecological Monographs 81, 169–193 (2012).
Mariotti, G. & Fagherazzi, S. Critical width of tidal flats triggers marsh collapse in the absence of sea-level rise. Proceedings of the National Academy of Sciences 110, 5353–5356, https://doi.org/10.1073/pnas.1219600110 (2013).
Fagherazzi, S. et al. Marsh collapse does not require sea level rise. Oceanography 26, 70–77 (2013).
Smith, S. M. et al. (2017) Hypsometry of Cape Cod Salt Marshes (Massachusetts, USA) and Predictions of Marsh Vegetation Responses to Sea-Level Rise. Journal of Coastal Research 537–547 (2017).
Thorne, K. et al. U.S. Pacific coastal wetland resilience and vulnerability to sea‐level rise. Science Adv 4, eaao3270 (2018).
Chapman, V. J. Salt marshes and salt deserts of the world. Wiley Interscience, New York, New York, USA (1960).
Nixon, S. W. The ecology of New England high salt marshes: a community profile. United States Department of Interior, Washington D.C., USA (1982).
Bertness, M. D. & Ellison, A. M. Determinants of pattern in a New England salt marsh plant community. Ecological Monographs 57, 129–147 (1987).
Hacker, S. D. & Bertness, M. D. Experimental evidence for factors maintaining plant species diversity in a New England salt marsh. Ecology 80, 2064–2073 (1999).
Bertness, M. D. Zonation of Spartina patens and Spartina alterniflora in a New England salt marsh. Ecology 72, 138–148 (1991).
Bertness, M. D. et al. Flood tolerance and the distribution on Iva frutenscens across New England salt marshes. Oecologia 91, 171–178 (1992).
Pennings, S. C. & Moore, D. J. Zonation of shrubs in western Atlantic salt marshes. Oecologia 126, 587–594 (2001).
Warren, R. S. & Niering, W. A. Vegetation change on a northeast tidal marsh: interactions of sea-level rise and marsh accretion. Ecology 74, 96–103 (1993).
Donnelly, J. P. & Bertness, M. D. Rapid shoreward encroachment of salt marsh cordgrass in response to accelerated sea-level rise. Proceedings of the National Academy of Sciences 98, 14218–14223 (2001).
Moody, R. M. et al. Effects of shoreline erosion on salt-marsh floral zonation. Marine Ecology Progress Series 488, 145–155 (2013).
Moeller, I. et al. Wind wave attenuation over saltmarsh surfaces: preliminary results from Norfolk, England. Journal of Coastal Research 12, 1009–1016 (1996).
Pringle, A. W. Erosion of a cyclic saltmarsh in Morecambe Bay, North-west England. Earth Surface Processes and Landforms 20, 387–405 (1995).
Pratolongo, P. D. et al. Combined effects of waves and plants on a mud deposition event at a mudflat-salt marsh edge in the Bahía Blanca Estuary. Estuarine Coastal and Shelf Science 87, 207–212 (2010).
Minchinton, T. E. Disturbance by wrack facilitates spread of Phragmites australis in a coastal marsh. Journal of Experimental Marine Biology and Ecology 281, 89–107 (2002).
Huston, M. A general hypothesis of species diversity. American Naturalist 113, 81–101 (1979).
Phillips, J. D. Spatial analysis of shoreline erosion, Delaware Bay, New Jersey. Annual Association of American. Geography 76, 50–62 (1986).
Schwimmer, R. A. Rates and Processes of Marsh Shoreline Erosion in Rehoboth Bay, Delaware, USA. Journal of Coastal Research 17, 672–683 (2001).
Marani, M. et al. Vegetation engineers marsh morphology through multiple competing stable states. Proceedings of the National Academy of Sciences USA 110, 3259–3263 (2013).
Da Lio, C. et al. The secret gardener: vegetation and the emergence of biogeomorphic patterns in tidal environments. Philos. Trans. R. Soc. Math. Phys. Eng. Sci. 371, 20120367, https://doi.org/10.1098/rsta.2012.0367 (2013).
Jiang, J. et al. Defining the next generation modeling of coastal ecotone dynamics in response to global change. Ecol. Model., Next generation ecological modelling, concepts, and theory: structural realism, emergence, and predictions 326, 168–176, https://doi.org/10.1016/j.ecolmodel.2015.04.0 (2016).
NOAA. Tides and Currents, Sea Level Trends, Lewes, Delaware, https://tidesandcurrents.noaa.gov/sltrends/sltrends_station.shtml?id=8557380 (2018).
Pijanowski, K. Patterns and Rates of Historical Shoreline Change in the Delaware Estuary. MS Thesis, University of Delaware 109 pp (2016).
Wijte, H. B. M. & Gallagher, J. L. Effect of oxygen availability and salinity on early life history stages of salt marsh plants. I. Different germination strategies of Spartina alterniflora and Phragmites australis (Poaceae). American Journal of Botany 83, 1337–1342 (1996).
Holdridge, L. R. Life Zone Ecology. Tropical Science Center, San Jose, Costa Rica (1967).
Jerolmack, D. J. et al. Internal boundary layer model for the evolution of desert dune fields. Nature Geoscience 5, 206–209 (2012).
Silvertown, J. The evolutionary maintenance of sexual reproduction: evidence from the ecological distribution of asexual reproduction in clonal plants. International Journal of Plant Science 169, 157–168 (2008).
Fenner, M. & Thompson, K. The ecology of seeds. Cambridge University Press, Cambridge, UK (2005).
Leck, M. A. et al. Seedling Ecology and Evolution. Cambridge University Press, Cambridge, UK (2008).
Kettenring, K. M. Mechanisms of Phragmites australis invasion: feedbacks among genetic diversity, nutrients, and sexual reproduction. Journal of Applied Ecology 48, 1305–1313 (2011).
McCormick, M. K. et al. Extent and reproductive mechanisms of Phragmites australis spread in brackish wetlands in Chesapeake Bay, Maryland (USA). Wetlands 30, 67–74 (2010).
Baldwin, A. H. et al. Seed banks of Phragmites australis-dominated brackish wetlands: relationships to seed viability, inundation, and land cover. Aquatic Botany 93, 163–169 (2010).
Phillips, J. D. Shoreline processes and establishment of Phragmites australis in a coastal plain estuary. Vegetatio 71, 139–144 (1987).
Roman, C. T. et al. Salt marsh vegetation change in response to tidal restriction. Environmental Management 8, 141–150 (1984).
Reimold, R. J. et al. The Effects of Smothering a Spartina alterniflora Salt Marsh with Dredged Material. U.S. Army Corps of Engineers Technical Report D-78-38, Waterways Experiment Station, Vicksburg, MS (1978).
Walters, D. C. & Kirwan, M. L. Optimal hurricane overwash thickness for maximizing marsh resilience to sea level rise. Ecology and Evolution 6, 2948–2956 (2016).
Macreadie, P. I. et al. Loss of ‘blue carbon’ from coastal salt marshes following habitat disturbance. Plos One 8, e69244 (2013).
Ranwell, D. S. Spartina salt marshes in S. England. II. Rates and seasonal pattern of sediment accretion. Journal of Ecology 52, 79–94 (1964).
Wilson, K. R. et al. Stratigraphic and ecophysical characterizations of salt pools: dynamic landforms of the Webhannet Salt Marsh, Wells, Maine, USA. Estuaries and Coasts 32, 855–870 (2009).
Poppema, D. W. et al. Experiment-supported modelling of salt marsh establishment. Ocean Coast. Manag. 168, 238–250, https://doi.org/10.1016/j.ocecoaman.2018.10.039 (2019).
Grime, J. P. Competitive exclusion in herbaceous vegetation. Nature 242, 344–347 (1973).
Violle, C. et al. Experimental demonstration of the importance of competition under disturbance. Proceedings of the National Academy of Sciences 107, 12925–12929 (2010).
Chesson, P. & Huntly, N. The roles of harsh and fluctuating condition in the dynamics of ecological communities. The American Naturalist 150, 519–553 (1997).
Smith, K. R. et al. Effects of natural and anthropogenic change on habitat use and movement of endangered salt marsh harvest mice. Plos One 9, e108739 (2014).
Phillips, J. D. Coastal submergence and marsh fringe erosion. Journal of Coastal Research 2, 427–436 (1986).
Weil, C. B. Sediments, structural framework and evolution of Delaware Bay, a transgressive estuarine delta. Delaware Sea Grant 4–77, Newark (1977).
Fletcher, C. H. III. et al. Holocene depocenter migration and sediment accumulation in Delaware Bay: a submerging marginal marine sedimentary basin. Marine Geology 103, 165–183 (1992).
Gibbs, R. J. et al. Size of flocs suspended in Delaware Bay. Canadian Journal of Fisheries and Aquatic Sciences 40, s102–s104 (1983).
Neumann, M. & Starlinger, F. The significance of different indices for stand structure and diversity in forests. Forest Ecology and Management 145, 91–106 (2001).
Acknowledgements
This research was funded by NSF Coastal SEES 1325466. We would like to thank T. Curran, F. Rahman, S. Klein, P. Zelanko, E. Powell, T. Smith, R. Searfoss, A. Jugan, A. Yumaguchi, L. Perez, G. Barren, J. Farmer, I. Griffith, C. Vito, H. Oakland, S. Dench, M. Gentry, J. Krause, S. Courtney, and D. Wolfinger for field and laboratory assistance. Thank you to W.T. Quirk for fabrication of field equipment. We appreciate the helpful comments of an anonymous reviewer.
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T. Elsey-Quirk collected field data, analyzed the data, and wrote the manuscript. K. Raper collected and processed field data. K. Valentine analyzed bay-wide edge retreat and ridge migration rates and developed the model. G. Mariotti developed the model and wrote the manuscript.
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Elsey-Quirk, T., Mariotti, G., Valentine, K. et al. Retreating marsh shoreline creates hotspots of high-marsh plant diversity. Sci Rep 9, 5795 (2019). https://doi.org/10.1038/s41598-019-42119-8
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DOI: https://doi.org/10.1038/s41598-019-42119-8
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